2026-04-27T12:55:19Zhttps://uvadoc.uva.es/oai/request

oai:uvadoc.uva.es:10324/214812021-06-23T10:23:34Zcom_10324_1159com_10324_931com_10324_894col_10324_1310

Méndez, Francisco Richaud, Arlette Alonso Martín, Julio Alfonso 2016-12-07T19:00:40Z 2016-12-07T19:00:40Z 2015 Organic Letters, 2015, Vol. 17, p. 767 – 769 1523-7060 http://uvadoc.uva.es/handle/10324/21481 10.1021/ol5034628 767 769 Organic Letters 17 The Brønsted–Lowry and Lewis basicity dichotomy in the elimination vs substitution reaction competition is analyzed in terms of a novel Brønsted–Lowry–Lewis basicity ωp/e. This new index unifies the dichotomy and explains the competition between elimination and substitution mechanisms of alkyl centers with para-substituted phenols. eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ Attribution-NonCommercial-NoDerivatives 4.0 International Química analítica Elimination vs Substitution Reaction. A dicotomy between Bronsted-Lowry and Lewis basicity info:eu-repo/semantics/article